FDA Inspection 1100722 — Pentagon Blood Collection Site

Pentagon Blood Collection Site — FEI 3010596305

The FDA completed an inspection of Pentagon Blood Collection Site on August 22, 2019 in Washington, DC. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
August 22, 2019
Fiscal Year
2019
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Washington, DC (United States)

Citations

IDCFRDescription
1809321 CFR 630.10(g)(1)Proof Of Identity
1813321 CFR 640.21(f)Deferral due to rbc loss